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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06008535
Other study ID # TartuUH_Surgery Clinic
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 22, 2018
Est. completion date December 31, 2023

Study information

Verified date April 2024
Source Tartu University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main goal of the research is to evaluate the long-term results of open anterior alloplasty of inguinal hernia, mainly the occurrence of recurrences. The secondary aim of the study is to clarify the incidence of chronic pain and foreign body sensation 10 years after inguinal hernia surgery. Patients who meet the criteria for inclusion in the study are invited to an appointment, where a questionnaire is filled out, an clinical examination and an ultrasound examination are performed.


Recruitment information / eligibility

Status Completed
Enrollment 234
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - primary inguinal hernia operated between 2008-2013 at the Tartu University Hospital - elective surgery - age at least 18 years old at the time of the operation - ability to understand the guidelines and willing to participate in the study Exclusion Criteria: - recurrent hernia - strangulated hernia - age under 18 years at the time of surgery - does not agree to participate in the study - does not understand the guidelines. Regarding the last exclusion criterion: since it is an assessment of the remote results of the treatment and probably relatively many of the subjects are very elderly, it may happen that when contacting the patient by phone it turns out that the patient is no longer adequate to make a decision about participating in the study or to answer questions (experienced cerebral infarction, dementia, etc. .) - in this case, the patient is not invited to the appointment.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Open inguinal hernia repair
Lichtenstein hernioplasty or open inguinal hernia repair with self-gripping mesh

Locations

Country Name City State
Estonia Tartu University Hospital Tartu Tartumaa

Sponsors (1)

Lead Sponsor Collaborator
Tartu University Hospital

Country where clinical trial is conducted

Estonia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence Inguinal hernia recurrence on clinical examination or in ultrasound at 10-year follow-up
Secondary Chronic pain Chronic pain after open inguinal hernia repair. The pain questionnaire includes questions about pain at rest, on coughing, when rising from lying to sitting position and during physical effort and exercise (yes-or-no questions). If the answer to these questions are positive, then the pain is measured on visual analogue scale. at 10-year follow-up
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